Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
-/A | MAF: 0.12 (A)
Location

Chromosome 7: between 151573142 and 151573143 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs146040967, rs374204532

This variation has 10 HGVS names - click the plus to show

Variation displays